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Au400e

Manufactured by Beckman Coulter
Sourced in United States

The AU400e is a fully automated clinical chemistry analyzer designed for high-volume laboratories. It features a modular design and offers a range of analytical capabilities for a variety of clinical tests.

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Lab products found in correlation

6 protocols using au400e

1

Measuring Endocrine Disruptors in Urine

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Urine samples were shipped on dry ice to the NIEHS biorepository, where they were stored at −80 °C. We shipped frozen urine samples to the CDC in three batches. For women in the case-cohort study who did not develop UL during follow-up, we measured urinary concentrations in samples collected at baseline, 20 months, and 40 months. For incident UL cases detected during follow-up, we measured urinary concentrations in samples collected from baseline until the time point before UL detection. Urinary concentrations of BPA, BPF, and BPS; 2,4- and 2,5-dichlorophenol; benzophenone-3; triclocarban; triclosan; and methylparaben, ethylparaben, propylparaben, and butylparaben were quantified at the CDC using methods based on online solid-phase extraction coupled to high performance liquid chromatography-isotope dilution mass spectrometry (28 , 29 ). We followed strict Clinical Laboratory Improvement Amendments guidelines, including quality control materials and reagent blanks in each analytic run. Inter-batch precision varied by analyte and concentration, but was generally <7% (30 ). We measured urinary creatinine concentrations at NIEHS using a Beckman Coulter clinical analyzer AU400e.
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2

Lipid and Glucose Measurement Protocol

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As described previously [12 (link)], fasting serum concentrations of total cholesterol (TC), triacylglycerol (TG) and high-density lipoprotein-cholesterol (HDL-C) concentrations were measured using an AU 400e automated analyzer (Beckman Coulter, Brea, CA, USA) with enzymatic reagents (assay coefficient of variation <3%). LDL-C concentrations were calculated using the Friedewald equation [25 (link)]. Non-HDL-C was calculated using the following formula: TC-HDL-C. Very low-density lipoprotein-cholesterol (VLDL-C) concentrations were estimated by dividing TG concentrations (mmol/L) by 2.2. Fasting serum glucose concentrations were measured using an enzymatic method (Beckman Coulter).
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3

Serum Chemistry Analysis in CD-1 Mice

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Blood serum samples (approximately 50ul) from the female CD-1 offspring at PND 91 necropsies were collected for evaluation. The serum chemistry analyses (alkaline phosphatase, ALP; alanine aminotransferase, ALT; aspartate aminotransferase, AST; glucose, triglyceride, low-density lipoproteins, LDL; high-density lipoproteins, HDL, total bile acid, TBA; sorbitol dehydrogenase, SDH; and cholesterol) were determined using an Olympus AU400e (Beckman Coulter, Inc., Irving, TX) and reagents obtained from the instrument manufacturer (except LDL, HDL, and TBA – reagents obtained from Sekisui Diagnostics, LLC., Framingham, MA). Leptin and insulin immunoassays were performed in duplicate using a Sector Imager 2400 (Meso Scale Discovery, Gaithersburg, MD) and multiplexed reagents obtained from the instrument manufacturer. Assays were carried out as directed by the manufacturer.
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4

Serum Enzymes Reveal Liver Injury

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The activity of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), and sorbitol dehydrogenase (SDH) were used as an indicator of hepatocellular damage. Blood was collected from the retro-orbital vein of the eye under anesthetization, stored at 4 °C overnight, and then centrifuged at 1,500 Xg at 4 °C for 5 minutes. Serum was collected and stored at −70 °C prior to analysis. We determined the levels of ALT by using a detection kit from Sigma-Aldrich (St. Louis, MO, USA). AST detection kit was purchased from Beckman Coulter (Melville, NY, USA). SDH detection kit was purchased from Sekisui Diagnostics (Framingham, MA, USA). Both AST and SDH were measured using the Olympus AU400e clinical analyzer Beckman Coulter (Irving, TX, USA). A portion of liver was fixed in 4% neutral formaldehyde, processed, and stained with hematoxylin and eosin (H&E) to examine liver injury by morphological changes.
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5

Maternal-Fetal Lipid Metabolism Profiling

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Serum samples from dams and plasma samples from pups were analyzed for cholesterol and triglycerides using an Olympus AU400e clinical analyzer (Beckman Coulter Inc. Irving, TX).
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6

Lipid Profile Analysis Protocol

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Serum and milk samples were stored at -70°C until analyses were done. Total Triglycerides and Cholesterol kits were purchased from Beckman Coulter (Melvill, NY) and the non-esterified fatty acid (NEFA) kit was purchased from Sekisui Biagnostics (Exton, PA) according to manufacturer’s instructions. Samples were run in duplicate and analysis was performed using an Olympus AU400e (Beckman Coulter, Inc., Irving, TX).
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